Lista de obras -

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma

artículo científico publicado en 2011

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A genome-wide association study of DSM-IV cannabis dependence

artículo científico publicado en 2010

A genome-wide association study of alcohol dependence

artículo científico publicado en 2010

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

artículo científico publicado en 2009

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

artículo científico publicado en 2015

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

artículo científico publicado en 2012

Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian Genomics

artículo científico publicado en 2015

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

artículo científico publicado en 2016

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

CHRNB3 is more strongly associated with Fagerström test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results

artículo científico publicado en 2012

Centers for Mendelian Genomics: A decade of facilitating gene discovery

artículo científico publicado en 2022

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study

artículo científico publicado en 2017

Copy number variation in familial Parkinson disease

artículo científico publicado en 2011

Correction: Novel Genetic Locus Implicated for HIV-1 Acquisition with Putative Regulatory Links to HIV Replication and Infectivity: A Genome-Wide Association Study

artículo científico publicado en 2015

Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14

artículo científico publicado en 2005

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

artículo científico publicado en 2010

Genome-wide association analysis of ischemic stroke in young adults

artículo científico publicado en 2011

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

artículo científico publicado en 2010

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

artículo científico publicado en 2008

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

artículo científico publicado en 2017

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

artículo científico publicado en 2008

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).

artículo científico publicado en 2013

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

artículo científico publicado en 2012

Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association study

artículo científico publicado en 2015

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

artículo científico publicado en 2011

Quality control and quality assurance in genotypic data for genome-wide association studies

artículo científico publicado en 2010

Quality control procedures for genome-wide association studies

artículo científico publicado en 2011

Lista de obras de

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

A genome-wide association study of DSM-IV cannabis dependence

A genome-wide association study of alcohol dependence

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian Genomics

Association analysis identifies 65 new breast cancer risk loci.

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

CHRNB3 is more strongly associated with Fagerström test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results

Centers for Mendelian Genomics: A decade of facilitating gene discovery

Characterization of large structural genetic mosaicism in human autosome

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study

Copy number variation in familial Parkinson disease

Correction: Novel Genetic Locus Implicated for HIV-1 Acquisition with Putative Regulatory Links to HIV Replication and Infectivity: A Genome-Wide Association Study

Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

Genome-wide association analysis of ischemic stroke in young adults

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association study

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Quality control and quality assurance in genotypic data for genome-wide association studies

Quality control procedures for genome-wide association studies